Package 69367-214-01

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 69367-214-01
Digits Only 6936721401
Product NDC 69367-214
Description

100 TABLET in 1 BOTTLE, PLASTIC (69367-214-01)

Marketing

Marketing Status
Marketed Since 2019-05-21
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40a3c918-199c-482d-956d-4fbd42adcde9", "openfda": {"upc": ["0369367214018", "0369367213011"], "unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["d8a5874a-5ea7-456c-87d4-95b3188abc9b"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (69367-214-01)", "package_ndc": "69367-214-01", "marketing_start_date": "20190521"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (69367-214-10)", "package_ndc": "69367-214-10", "marketing_start_date": "20190521"}], "brand_name": "Phenobarbital", "product_id": "69367-214_40a3c918-199c-482d-956d-4fbd42adcde9", "dosage_form": "TABLET", "product_ndc": "69367-214", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "97.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20190521", "listing_expiration_date": "20261231"}